M5 Keratin 18
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The dead cells still count!™ Store at 2–8 °C For life science research only. Not for use in diagnostic procedures. FOR IN VITRO USE ONLY. M5 Keratin 18 200 tests (Peviva Prod. No. 10600) Mouse monoclonal antibody (Clone M5) For the detection of keratin 18 1. Product Description 2. Background Information Name: M5 Keratin 18 monoclonal antibody Clone: M5 2.1 Keratins Isotype: Mouse IgG2b Immunogen: Keratin 18 (K18) fragments purified from human carcinomas. In eukaryotic cells, the cytoskeleton is composed of three different types Epitope: Internal on K18 fragment aa284-396. of morphologically distinct filamentous structures: microfilaments, inter- mediate filaments (IF), and microtubules. The integrated cytoskeletal 1.1 Formulation network formed by the three filament systems is responsible for the me- chanical integrity of the cell and is a critical participant in several cellular Clear solution. 20 µg of M5 Keratin 18 antibody provided in 200 µl PBS con- processes, such as cell division, motility, and cell–cell contact. taining 0.1 % BSA, PEG, sucrose and 0.09 % sodium azide. For the intermediate filament (IF) protein family, a classification system divided into several groups has been implemented that is based on their 1.2 Specificity characteristics such as sequence similarities and patterns of expression. In- M5 Keratin 18 antibody recognises an internal formalin-resistant epitope termediate filament types I and II constitute the keratins (acidic and basic on human and monkey keratin 18 (K18) cytoskeletal protein. proteins, respectively), while the type III IF group includes desmin, vimen- tin, and glial fibrillary acidic proteins. Type IV includes the neurofilament 1.3 Recommended applications proteins (NF-L, NF-M, and NF-H) and internexin, while type V proteins are known as nuclear lamins, exclusive to the cell nuclei. The remaining IF pro- • Immunocytochemistry (ICC) teins, sometimes called type VI, include filensin and phakinin. • Flow cytometry (FACS) • Western blot (WB) The epithelial keratins (IF types I and II) are conserved phylogenetically and • Immunoprecipitation (IP) are closely related, biochemically and immunologically. Keratins 1–8 con- • Immunohistochemistry (IHC) including formalin-fixed and paraffin- stitute the type II group (53–68 kDa, neutral to basic protein components), embedded tissue (FFPE) and cryostat/frozen sections (FS). while keratins 9–20 constitute the type I group (40–56 kDa, acidic proteins). This dual nature of the keratins is functionally important as the keratin pro- 1.4 Working solution teins assemble into obligate non covalent heterodimers containing one keratin protein of type I and one keratin protein of type II (such as keratins 8 M5 Keratin 18 antibody is provided in a convenient stock solution. Use a and 18) in stochiometric amounts [1–3]. dilution 1:100 in Incubation Buffer (final concentration 1.0 µg/ml). 2.2 Keratins as biomarkers in epithelial cancer 1.5 Storage and stability Keratins, belonging to the intermediate filament (IF) protein family, are The M5 Keratin 18 antibody is provided in a ready-to-use format and is sta- particularly useful tools in oncology diagnostics. More than 20 different ble at 2–8 °C through the expiration date printed on the label. Alternatively, keratins have been identified, of which keratins 8, 18, and 19 are the most it can be stored in aliquots at -20 °C. The antibody is shipped at ambient abundant in simple epithelial cells. Upon release from dying cells, keratins temperature. provide useful markers for epithelial malignancies, distinctly reflecting on- Note: Repeated freezing and thawing should be avoided. going cellular turnover. Certain keratins, the most prominent example being keratin 18, are sub- 1.6 Quality control strates for lethal caspase activation and the subsequent release of defined The M5 Keratin 18 antibody is function tested using a cellular model: HeLa protein fragments occurs during apoptotic cell death. The clinical value of cells analysed by immunocytochemistry and flow cytometry. FFPE tissue determining different soluble keratin protein fragments in body fluids lies sections obtained from human prostate cancer analysed by immunohisto- in the early detection of recurrence and the fast assessment of the efficacy chemistry. of therapy response in epithelial cell carcinomas [4-7]. M5 Keratin 18 Antibody – Overview 2.3 Keratins during apoptosis and necrosis The morphological features of apoptosis such as cell shrinkage, nuclear Benefits Features fragmentation, and apoptotic body formation arise from the cleavage of specific cellular (“death”) substrates by caspases. Exceptional broad range of appli- Suitable for WB, IP, ICC, IHC (PS/FS) , cations, including FFPE. FC on endogenous native K18. Specific to apoptosis, one consequence of this cleavage is the exposure of a C-terminal neo-epitope (at cleavage site Asp396) in keratin 18 (designated Specificity for simple epithelial (i.e Expression pattern of K18 is re- “M30”), which is not present in the keratin 8/18 complex in vital or necrotic carcinoma) cells and tissue. stricted to cells of epithelial origin. epithelial cells. The biological significance of keratin cleavage during apop- Lymphoid, fibroblast and neuronal tosis is not fully understood, although it has been suggested that caspase cells are not detected by M5 Kera- cleavage of the keratin proteins is likely to facilitate the formation of apop- tin 18 antibody. totic bodies and amplify the apoptotic signal. In vitro experiments have shown that cellular release of keratin 18 fragments into the extracellular space occurs as a consequence of caspase cleavage and thereby can serve as markers of apoptosis, using the M30 Cyto DEATH™ antibody or the M30 Apoptosense® ELISA [8–12]. 3. Procedures and Materials required 3.1.2 Immunohistochemistry protocol Note: For optimal results it is recommended to follow the method for anti- 3.1 Procedure for immunohistochemistry gen retrieval described in the table below. 3.1.1 Introduction Step Action The following procedure describes the detection of K18 with M5 Keratin 18 1 Autoclave tissue section slides 10 min at 121 °C. antibody in immunohistochemistry for paraffin-embedded tissue in a three Let cool down in antigen retrieval buffer 30 min at 15–25 °C. step method for maximal sensitivity. Place in PBS plus 0.05 % Tween® 20 for 10 min at 15–25 °C. If using other detection methods or sample material, conditions may vary 2 Incubate with blocking solution i.e. PBS containing 5 % normal and may have to be adapted. serum (i.e. from goat, if secondary antibody from goat). Preparation of working solutions 3 Remove blocking solution and add 100 µl M5 Keratin 18 antibody working solution for 30 min at 15–25 °C in a humid The following table lists the working solutions needed to perform the chamber. immuno histochemistry staining procedure. 4 Wash slides in Washing Buffer (use 3 separate jars and dip Working solution Composition Stability Storage 3 × into each jar). PBS containing 5 Cover the section with 100 µl of anti-mouse-IgG biotin accord- Washing Buffer 4 weeks at 2–8 °C 0.05 % Tween® 20 ing to your preferred optimised procedure for the reagent from your selected supplier. Incubate for 30 min at 37 °C in a PBS containing Incubation Buffer 4 weeks at 2–8 °C humid chamber. 1 % BSA 6 Wash slides in Washing Buffer (use 3 separate jars and dip Tris 10 mM, pH 9.0 Antigen retrieval 4 weeks at 2–8 °C 3 × into each jar). 0.05 % Tween® 20 7 Cover the section with 100 µl of streptavidin-POD according Preparation of antibody working solution to your established optimised procedure for the reagent from your selected supplier (i.e. ABC reagent from Vectorlabs). Incu- Dilute M5 Keratin 18 antibody stock solution 1:100 in Incubation Buffer bate for 30 min at 15–25 °C in a humid chamber. (final concentration 1.0 µg/ml). 8 Wash slides in Washing Buffer (use 3 separate jars and dip Note: The antibody solutions should be free of precipitate; if necessary, 3 × into each jar). Dehydrate depending on used substrate, i.e. centrifuge vial at high speed prior to use. for DAB. Preparation of sample material 9 Incubate slides in a freshly prepared substrate solution (i.e. AEC) at 15–25 °C until a clearly visible colour develops Before starting the immunohistochemical protocol, dewax paraffin- (1–5 min). A negative control should not show any develop- embedded tissue sections as described in the following table. ment of colour during the incubation period. Step Action 10 Stop the reaction by extensive rinsing in double distilled water. 1 Place paraffin-embedded sections into an incubator at 37 °C 11 Subsequently, counterstain the preparation and mount sec- over night to air-dry. tions i.e. in Aquatex for AEC, or in Vectamount for DAB. 2 For deparaffinisation of FFPE tissue slides, process as follows at 15–25 °C for 3 min each: 3 × in xylol 3.1.3 Immunohistochemistry results 2 × in ethanol (96 %) 1 × in ethanol (80 %) A B 1 × in methanol freshly prepared with H2O2 (3 %) for 10 min. 3 Rinse 3 × for 10 min in PBS containing 0.05 % Tween® 20. Note: The sections should not be allowed to dry during this procedure. Figure: A. Detection of K18 in formalin-fixed and paraffin-embedded (left panel) or frozen (right panel) section from a human prostate tissue showing confined epithelial staining for K18 with M5 Keratin 18. Secondary detec- tion with anti-mouse IgG-biotin, streptavidin-POD and DAB as subtrate. B. Frozen section from a human prostate tissue shows confined staining for K18 in epithelial cells using M5 Keratin 18 (left panel) and nuclear coun- terstain with DAPI (right panel). Secondary detection with anti-mouse IgG -ALEXA-488. Images by courtesy of Claudia Strele, Tissuegnostics, Vienna, Austria. 3.2 Procedure for immunofluorescence and flow cytometry 5. References 3.2.1 Introduction 1.